Canonical Allele Identifier: CA1879828448
Gene: LRSAM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127501013T= , CM000671.2:g.127501013T= GRCh38
NC_000009.11:g.130263292T= , CM000671.1:g.130263292T= GRCh37
NC_000009.10:g.129303113T= NCBI36
NG_032008.1:g.54528T= , LRG_373:g.54528T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300417.11:c.1916T= MANE Select ENSP00000300417.6:p.Leu639=
ENST00000472068.2:c.*1640T= ENSP00000501555.1:n.*1640T=
ENST00000483302.6:n.2581T=
ENST00000498513.6:c.*807T= ENSP00000501637.1:n.*807T=
ENST00000674511.1:n.1515T=
ENST00000674516.1:c.*532T= ENSP00000502441.1:n.*532T=
ENST00000674621.1:n.1861-2360T=
ENST00000674771.1:c.*559T= ENSP00000502627.1:n.*559T=
ENST00000674784.1:c.*976T= ENSP00000501837.1:n.*976T=
ENST00000674970.1:c.*1690T= ENSP00000502493.1:n.*1690T=
ENST00000675012.1:n.1860T=
ENST00000675141.1:c.1817T= ENSP00000502420.1:p.Leu606=
ENST00000675198.1:n.1796T=
ENST00000675213.1:c.1871T= ENSP00000502218.1:p.Leu624=
ENST00000675224.1:c.1944T= ENSP00000501869.1:p.Ala648=
ENST00000675253.1:c.*588T= ENSP00000502557.1:n.*588T=
ENST00000675445.1:c.*1588T= ENSP00000502253.1:n.*1588T=
ENST00000675448.1:c.1916T= ENSP00000502167.1:p.Leu639=
ENST00000675521.1:n.1826T=
ENST00000675572.1:c.1817T= ENSP00000501598.1:p.Leu606=
ENST00000675641.1:c.*658T= ENSP00000501845.1:n.*658T=
ENST00000675657.1:c.*529T= ENSP00000502002.1:n.*529T=
ENST00000675662.1:n.1711T=
ENST00000675789.1:c.1736T= ENSP00000501954.1:p.Leu579=
ENST00000675883.1:c.1835T= ENSP00000501592.1:p.Leu612=
ENST00000675945.1:c.*557T= ENSP00000501835.1:n.*557T=
ENST00000676014.1:c.1859T= ENSP00000502058.1:p.Leu620=
ENST00000676035.1:n.1578T=
ENST00000676106.1:n.1953T=
ENST00000676137.1:n.1946T=
ENST00000676170.1:c.1997T= ENSP00000502177.1:p.Leu666=
ENST00000676318.1:c.*2746T= ENSP00000502300.1:n.*2746T=
ENST00000676336.1:c.*529T= ENSP00000502686.1:n.*529T=
ENST00000676349.1:c.*1604T= ENSP00000502155.1:n.*1604T=
ENST00000676399.1:n.1819T=
ENST00000676409.1:n.1976T=
ENST00000300417.10:c.1916T= ENSP00000300417.6:p.Leu639=
ENST00000323301.8:c.1916T= ENSP00000322937.4:p.Leu639=
ENST00000373322.1:c.1916T= ENSP00000362419.1:p.Leu639=
ENST00000373324.8:c.1835T= ENSP00000362421.4:p.Leu612=
ENST00000472068.1:n.809T=
ENST00000483302.5:n.1138T=
NM_001005373.3:c.1916T= NP_001005373.1:p.Leu639=
NM_001005374.3:c.1916T= NP_001005374.1:p.Leu639=
NM_001190723.2:c.1835T= NP_001177652.1:p.Leu612=
NM_138361.5:c.1916T= , LRG_373t1:c.1916T= NP_612370.3:p.Leu639=
XM_006717316.2:c.1817T= XP_006717379.1:p.Leu606=
XM_006717316.4:c.1817T= XP_006717379.1:p.Leu606=
XM_017015283.1:c.1916T= XP_016870772.1:p.Leu639=
XM_017015284.2:c.1127T= XP_016870773.1:p.Leu376=
XR_001746415.2:n.2451T=
XR_929874.3:n.2275T=
NM_001190723.3:c.1835T= NP_001177652.1:p.Leu612=
NM_001005373.4:c.1916T= MANE Select NP_001005373.1:p.Leu639=
NM_001005374.4:c.1916T= NP_001005374.1:p.Leu639=
NM_001384142.1:c.1916T= NP_001371071.1:p.Leu639=
NM_001384143.1:c.1817T= NP_001371072.1:p.Leu606=
NM_001384144.1:c.1127T= NP_001371073.1:p.Leu376=
NR_168891.1:n.2445T=
NR_168892.1:n.2269T=